重度再生障碍性贫血(SAA)的骨髓移植(BMT)后妊娠和分娩。一份病例报告。

M. Hinterberger‐Fischer, W. Hinterberger, A. Hayek-Rosenmayr, P. Höcker, K. Wagner, H. Sewann, K. Lechner
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引用次数: 2

摘要

摘要一例23岁的重度再生障碍性贫血(SAA)患者接受了骨髓移植手术。用环磷酰胺(200mg /kg)进行调理,给予供体灰白色被细胞预防排斥反应。BMT后7个月,在没有外源性激素操纵的情况下,患者开始正常月经,BMT后21个月,患者怀孕。妊娠第14周出现腮腺炎并发症。它是通过剖宫产终止的。正常发育的新生女婴(3450克)表现为“持续性胎儿循环综合征”。手术矫正博塔利动脉导管未闭后,女婴恢复迅速。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pregnancy and delivery after bone marrow transplantation (BMT) for severe aplastic anemia (SAA). A case report.
A 23 years old multiple pretransfused female with severe aplastic anemia (SAA) underwent bone marrow transplantation (BMT). Cyclophosphamide (200 mg/kg) was used for conditioning, donor buffy coat cells were given as rejection prophylaxis. Seven months after BMT regular menses started in the absence of exogenous hormonal manipulation and 21 months after BMT the patient became pregnant. Pregnancy was complicated by mumps in the 14th week. It was terminated at term by cesarean section. The normally developed newborn girl (3,450 gm) presented with a "persistent fetal circulation syndrome". After surgical correction of the patent ductus arteriosus Botalli the girl baby recovered quickly.
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